Esters of alpha-hydroperoxy-bis-p-halophenylacetic acids

ABSTRACT

A PROCESS FOR TH PREPARATION OF ESTERS OF A-HYDROPEROXY-BIS-P-CHLORO-(OR-BROMO)-PHENYLACETIC ACIDS, COMPOSITIONS CONTAINING SUCH MATERIALS AND NEW ESTERS OF A-HYDROPEROXY-BIS-P-BROMO-PHENYLACETIC ACIDS ARE DISCLOSED.

United States Patent 3,773,811 ESTERS OF oc-HYDROPEROXY-BIS-P-HALO- PHENYLACETIC ACIDS Yair Sprinzak, Rehovoth, Israel, assignor to Yeda Re- ABSTRACT OF THE DISCLOSURE A process for the preparation of esters of a-hydroperoxy-bis-p-chloro-(or-bromo)-phenylacetic acids, compositions containing such materials and new esters of u-hydroperoxy-bis-p-bromo-phenylacetic acids are disclosed.

FIELD OF THE INVENTION The present invention relates to esters of the a-hydroperoxy-bis-p-chloro-(or-bromo)-phenylacetic acids.

SUMMARY OF THE INVENTION The present invention relates to esters of the following formula:

in which R is chloro or bromo and R may be an alkyl radical having preferably from 1 to 5 carbon atoms and including both unsubstituted and substituted groups, e.g. methyl, ethyl, i-propyl, n-butyl, s-butyl, n-amyl; an allyl radical' including both unsubstituted and substituted allyl groups; a cycloalkyl radical having preferably from 5 to 7 carbon atoms in the nucleus thereof and including both unsubstituted and substituted groups, e.g. cyclohexyl; an aryl radical including both unsubstituted and substituted 'aryl groups; and an aralkyl radical having preferably from 1 to 3 carbon atoms in the alkyl chain thereof and including both unsubstituted and substituted aralkyl groups, e.g. benzyl.

The esters of Formula I are suitable agents for destroying vermin and, in particular, are excellent acaricides. Thus, for example, it has been found that various of such esters are very effective against rust mites, common red mites and citrus bud mites. The esters may be applied alone to the plants or the soil or they may be formulated on granules for application with a conventional fertilizer spreader, as an emulsifiable concentrate or a wettable powder for application as dilute sprays, as a dust for application with a conventional duster, or adsorbed on activated carbon for application on seeds.

The acaricidal compounds hereof are effective when employed in dilute concentrations. It is preferred, therefore, to incorporate the compounds in a variety of suitable solid or liquid carriers or diluents. Such compositions can be prepared either as a suspension in a suitable non-solvent or a dust. A suspension or dispersion of the acaricidal compound in a non-solvent such as water may be prepared for direct application to infested plants or soil. Alternatively, a prepared suspension of the compound may be modified by the addition thereto of a commercially available dispersing or surface agent. Examples of surface active compounds so useful are: An ethylene oxide "Ice condensate nonionic emulsifier; alkyl aryl sulfonates, e.g. calcium dodecyl benzene sulfonate.

In the preparation of dusts, the acaricidal compound may be admixed with a finely divided inert granular material as a carrier in any conventional manner. ."Useful carriers include kaolin, bentonite, talc. pumice, silica, chalk, wood flour, fullers earth, activated carbon, charcoal and the like.

The esters of Formula I-are also useful as chemical intermediates for use in the preparation of the following formula (II) (p-RCoHOzC-C 0 O R in which R and R have the same meaning as set forth above. The esters of Formula I can readily be converted into those of Formula II, which are known pesticides (see, for example, R. Gasser, Experientia, vol. VIII/2, p. (1952) by'way of reduction reactions.

The present invention also comprises a process for the preparation of esters of Formula I, which comprises oxidizing an ester of the following formula:

(III) (p-R'C H CHCOOR in which R and R have the same meaning as set forth above, with oxygen in an inert organic solvent and in the presence of a catalyst consisting essentially of asolid anhydrous alkali metal hydroxide and a small amount of alcohol.

acid esters useful as acaricides in accordance with the present invention are ethyl and isopropyl a-hy-droperoxybis-p-bromophenylacetate. These materials have been found to possess particularly eflicacy against a wide variety of mites, particularly rust mites, common red mites and citrus bud mites, as stated hereinabove.

The above novel esters and other esters of Formula I are prepared from the corresponding esters of Formula III. Such ester reactants are either known per se or may be prepared by esterification of the known acids. The reaction is, as previously noted, carried out in the presence of a catalyst consisting essentially of from about 0.25 to 0.75 part by weight of an anhydrous alkali metal hydroxide, e.g. lithium, sodium or potassium hydroxide (the latter being preferred) to 1 partrof the ester of Formula III,- and a suitable alcohol, e.g. a monohydric alkanol, such as methanol, ethanol, isopropanol, n-butanol or tbutanol in an amount corresponding to about 4 to 12% of the amount of the hydroxide.

The oxidation reaction is carried out in an inert organic solvent which should be inert to theinitial ester reactant -(of Formula III), to the catalyst, and to the reaction prod- .uct (of Formula I). The inert solvent should also effect dissolution of at least a substantial proportion of the ester reactant. As suitable solvents there may be men tioned aliphatic hydrocarbons, e.g. n-heptane; aromatic hydrocarbons, e.g. toluene; chlorinated hydrocarbons, e.g. chlorobenzene; ethers, e.g. isopropyl ether, tetrahydrofuran and the like. In the event that the solvent comprises an alcohol in whole or in part, the further alcohol component of the catalyst composition may be partially or entirely eliminated.

The synthesis of the esters hereof is preferably performed at temperatures below room temperature, advantageously at or below (All temperatures are indicated herein as degrees centigrade.)

The oxidation may be performed with any suitable oxidizing medium, e.g. with pure oxygen or with air.

The invention will be illustrated by the following specific examples but is not intended that the invention be limited in any manner by them.

Example 1 A mixture comprising 12.92 g. of isopropyl bis-p-chlorophenylacetate, 180 ml. of toluene, 8 g. of powdered anhydrous potassium hydroxide and 0.07 ml. of ethanol was kept at 0 and stirred in an atmosphere of oxygen whereupon absorption of oxygen took place. Another 0.07 ml. of ethanol was added when 120 ml. of oxygen had been absorbed, the total volume of oxygen absorbed amounting finally to one liter, the mixture being stirred as long as the oxygen absorption took place.

The supernatant liquid was poured into a dilute solution of sodium hydrogen carbonate, the organic layer was separated and washed with water, the toluene was distilled off under reduced pressure to yield 13.17 g. of crystalline isopropyl a-hydroperoxy-bis-p-chlorophenylacetate, M.P. 9597. On recrystallization from petroleum/ether, the product melted at 100-101". Analysis: C=57.65%; H=4.50%. Active oxygen: [O]=4.5%.

This compound is very effective against common red mites, rust mites and against citrus bud mites.

Against the common red mite after 24 hours LD was 0.009%.

The following experiment was performed to test the activity against rust mites:

Branches of Shamouti orange trees heavily populated with rust mites were sprayed with an emulsion of 0.03% isopropyl a-hydroperoxy bis p chlorophenylacetate. Counts made and 47 days after treatment revealed no mites on the treated branches, while infestation of the untreated branches remained high. Noburns or spots were observed in either fruit or leaves.

Example 2 The oxidation of isopropyl bis-p-chlorophenylacetate was carried out as described in Example 1, except that the ethanol was replaced by t-butyl alcohol.

6.46 g. of the acetate yielded 6.80 g. of the hydroperoxy acetate, M.P. 94-96. On recrystallization the product melted at 10010l.

Example 3 A mixture of 6.46 g. of isopropyl bis-p-chlorophenylacetate, 90 ml. of isopropyl ether and 4 g. of powdered, anhydrous potassium hydroxide was oxidized as described in Example 1. 0.2 ml. of ethanol was added to the mixture after 260 ml. of oxygen had been absorbed. The

total volume of oxygen absorbed amounted to 500 ml.

The reaction mixture was worked up in the same manner as described in Example 1. The yield and the quality of the product were the same as those described in Example 1.

Example 4 water, and evaporated to yield 6.22 g. of isopropyl a-hydroperoxy-bis-p-chlorophenylacetate. It was washed with 10 ml. of petroleum/ ether to yield 5.34 g. of the product, M.P. 9698. After recrystallization from petroleum/ ether, the product had a M.P. of l0010l.

Example 5 An oxidation was carried out as described in Example 1, utilizing as starting material n-butyl bis-p-chlorophenylacetate and as solvent n-heptane, and performing the oxidation at l7.

6.74 g. of the ester yielded 7.00 g. of n-butyl a-hydroperoxy-bis-p-chlorophenylacetate in the form of a thick oil. [O]=3.9%.

Example 6 An oxidation was carried out as described in Example 1, utilizing as starting material sec-butyl bis-p-chlorophenylacetate. 6.74 g. of the latter yielded 7.10 g. of crystalline sec-butyl a-hydroperoxy-bis-p-chlorophenylacetate, M.P. 9294. On recrystallization from petroleum/ether, the product melted at 96-97. Analysis: C=58.87%; H=4.88%. [O]=4.3%.

Example 7 An oxidation was carried out as described in Example 1, utilizing as starting material n-amyl bis-p-chlorophenylacetate, and performing the oxidation at 18. 7.02 g. of the latter yielded 7.50 g. of n-amyl a-hydroperoxy-bisp-chlorophenylacetate in the form of a thick oil. Analysis: C=59.53%; H=5.22%. [O]=3.9%.

Example 8 A mixture comprising 5.90 g. of methyl bis-p-chlorophenylacetate, ml. of chlorobenzene, 4 g. of powdered anhydrous potassium hydroxide and 0.3 ml. of ethyl alcohol was kept at 17 and stirred in an atmosphere of oxygen, whereby absorption of the gas took place. Stirring was continued to complete absorption, the total vol ume of oxygen absorbed amounting to 500 ml. at atmospheric pressure and ambient temperature.

The reaction mixture was worked up as described in Example 1 to yield 6.25 g. of methyl a-hydroperoxy-bisp chlorophenylacetate in the form of a thick oil. [0]: 4.3%.

EXAMPLE 9 A mixture of 6.18 g. of ethyl bis-p-chlorophenylacetate, 90 ml. of chlorobenzene and 4 g. of powdered, anhydrous potassium hydroxide, kept at -l8, was stirred in an atmosphere of oxygen while small quantities of ethanol were being added thereto in order to maintain the absorption of the gas. 0.8 ml. of ethanol were added, the volume of oxygen absorbed amounting to 500 ml.

The reaction mixture was worked up as described in Example 1, yielding 6.74 g. of ethyl a-hydroperoxy-bisp-chlorophenylacetate in the form of a thick oil. [0]: 4.3%.

This product is very effective against rust mites, common red mites and bud mites.

The following experiment was performed to test the activity against rust mites:

A tree of grape fruit heavily populated with rust mites was sprayed with an emulsion of 0.035% ethyl tat-hydroperoxy-bis-p-chlorophenylacetate. Counts made after 6 and 51 days after treatment revealed no mites on the treated branches, while infestation of the untreated branches remained high.

Example 10 An oxidation was carried out as described in Example 9, utilizing as starting material n-propyl bis-p-chlorophenylacetate and as solvent toluene. 6.46 g. of the above ester yielded 7.10 g. of n-propyl a-hydroperoxybis-p-chlorophenylacetate in the form of a thick oil. [O]=4.0%.

5. Example 11 A mixture comprising 7.68 g. of methyl bis-p-bromophenylacetate, 90 ml. of toluene, 4 g. of powdered anhydrous potassium hydroxide and 0.3 ml. of ethanol was Example 12 An oxidation was carriedout as described in Example 11, utilizing as starting material ethyl bis-p-bromophenylacetate, 7.96 g. of the ester yielded 8.52 g. of ethyl u-hydroperoxy-bis-p-bromophenylacetate in the form of a thick oil, which crystallized on treatment with petroleum/ ether, M.P. 52-54. [O]=3.7%.

Example 13 An oxidation was carried out as in Example 11, utilizing as staring material isopropyl bis-p-bromophenylacetate, and performing the oxidation at 8.24 g. of the ester yielded 8.74 g. of isopropyl a-hydroperoxy-bis-p-bromophenylacetate, M.P. 85-87. On recrystallization from petroleum/ ether the product melted at 88-89. Analysis: C=46.05%; H=3.57%. [O]=3.6%.

Against the common red mites after 24 hours the LD was 0.0052%.

Example 14 An oxidation of isopropyl bis-p-bromophenylacetate was carried out as in Example 11, utilizing as solvent chlorobenzene and performing the oxidation at 0. 8.24 g. of the ester yielded 8.75 g. of isopropyl a-hydroperoxybis-p-bromophenylacetate, M.P. 83-87, which on recrystallization from petroleum/ether melted at 88-89".

Example 15 An oxidation was carried out as in Example 11, utilizing as starting material isopropyl bis-p-bromophenylacetate and as solvent n-heptane, and performing the oxidation at 0. Isopropyl a-hydroperoxy-bis-p-bromophenylacetate was obtained in the same yield and quality as in Example 14.

Example 16 A solution of 8.24 g. of isopropyl bis-p-bromophenylacetate in 60 ml. of tetrahydrofuran was added to a mixture of 30 ml. of tetrahydrofuran and 4 g. of powdered anhydrous potassium hydroxide, kept at 18 and stirred in an atmosphere of oxygen. 460 ml. of oxygen were absorbed.

The supernatant liquid was poured into a dilute solution of sodium hydrogen carbonate and the product extracted with benzene, the organic layer was washed with water and evaporated to yield 8.05 g. of isopropyl whydroperoxy-bis-p-bromophenylacetate, M.P. 82-87", which on recrystallization from petroleum/ether melted at 88-89".

Example 17 An oxidation was carried out as in Example 11, utilizing as starting material allyl bis-p-bromophehylacetate.

8.20 g. of the ester yielded 8.80 g. allyl u-hydroperoxybis-p-bromophenylacetate in the form of a thick oil.

Example 18 An oxidation was carried out as in Example 11, utilizing n-butyl bis-p-bromophenylacetate as starting material.

8.52 g. of the ester yielded 8.90 g. n-butyl a-hydroperoxybis-p-bromophenyl acetate, M.P. 60-64, which after washing with petroleum/ether melted at 64.5-65.5. Analysis: C'= 47.24% H=3.81%. [0]=3.8%.

Example 19 An oxidation was carried out as in Example 11, utilizing sec-butyl bis-p-bromophenylacetate as starting material and isopropyl ether as solvent, and performing the oxidation at 0. 8.52 g. of the esteryielded 8.76 g. of sec-bu'tyl u-hydroperoxy-bis-p-bromophenylacetate, M.P. 92-94, which on recrystallization from petroleum/ether melted at 95-95.7. Analysis: C=47.33%; H=3.95%. [O =3.5%.

Example 20 An oxidation was carried out as in Example 11, utilizing as starting material n-amyl bis-p-bromophenylacetate. 8.80 g. of the ester yielded 9.08 g. of n-amyl u-hydroperoxy-bis-p-bromophenylacetate, M.P. 56-60", which after washing with petroleum/ ether, melted .at 66.5-67.5.

Example 21 An oxidation was carried out as in Example 1, utilizing as starting material cyclohexyl bis-p-chlorophenylacetate. 7.26 g. of the ester yielded 7.5 g. of cyclohexyl a-hydroperoxy-bisp-chlorophenylacetate, M.P. 9l-93. After recrystallization from petroleum/ether the product had a M.P. of 93.5-94.5". [O]=4.0%.

Example 22 An oxidation was carried out as in Example 1, utilizing as starting material benzyl bis-p-chlorophenylacetate and performing the oxidation at -18. 7.42 g. of the ester yielded 7.87 g. of benzyl a-hydroperoxy-bis-p-chlorophenylacetate in the form of a thick oil. [O]=3.7%.

What is claimed is:

1. An ester of the formula (p-RCaH4)zCGOOR OH in which R is ethyl or isopropyl; and R is a bromine atom.

2. The ester of claim 1, wherein R is ethyl.

3. The ester of claim 1, wherein R is isopropyl.

4. A process for the production of an ester of the formula (p-R'CaHOzC-C O O R in which R is alkyl having from 1 to 5 carbon atoms, alkyl, cycloalkyl having from 5 to 7 carbon atoms in the nucleus thereof, aryl, and aralkyl having from 1 to 3 carbon atoms in the alkyl chain thereof; and R is a chlorine or bromine atom, which comprises reacting an ester of the formula where R and R are as defined above, with oxygen in an inert organic solvent in the presence of a catalyst consisting essentially of a solid, anhydrous alkali metal hydroxide and about 4%-12% based on the hydroxide of an alcohol at temperatures at/or below 0.

5. The process of claim 4, in which R is alkyl.

6. The process of claim 4, in which R' is a chlorine atom.

7. The process of claim 4, in which R is a bromine atom.

8. The process of claim 4 wherein the alcohol is a monohydric alkanol and wherein the alcohol is employed in an amount of about 4-12% of the hydroxide.

9. The process of claim 8 wherein R is a bromine atom.

10. The process of claim 9 wherein R is ethyl.

11. The process of claim 9 wherein R is isopropyl.

12. Isopropyl u-hydroperoxy-bis-4-chlorophenylacetate.

(References on following page) References Cited UNITED STATES PATENTS Calhoun et a1 260-610 B Natta et a1. 260-610 B Fisher 260610 B Dressler et a1 260610 B Hennessey et a1. 260469 Green et a1 260-610 B Farkas et a1. 260610 B FOREIGN PATENTS 8 OTHER REFERENCES Chemistry & Industry, Jan. 6, 1962, Cullis, pp. 23-28.

Chem. Abs., 1955, 001. 387721, Ynfiester et a1.

Trudy Khirn and Khim Technical I, No. 3, 693-700 (1958) abs. Kolmakov.

LORRAINE A. WEINBERGER, Primary Examiner R. S. WEISSBERG, Assistant Examiner US. Cl. X.R. 424-308 Po-ww I UNITED sTATEs PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 3,773,811 Dated November 20 1973 Inventor(s) Yair Sprinzak It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:

1 F I I q Column 6, line 49, for "alkyl," read allyl,

Signed and sealed this 16th day of April 1971+.

(SEAL) Attest: v

EDWARD i'IJ LOZTGHEILJR. A C. WAR-SHALL DANN I Attesting Officer I Commissioner-"Of Patents 

